Rapid detection of specific messenger RNAs in thyroid carcinomas by reverse transcription-PCR with degenerate primers : Specific expression of oncofetal fibronectin messenger RNA in papillary carcinoma
The search for mRNAs that are specifically expressed in cancer tissues is important for gene diagnosis and therapy. However, finding such mRNAs in human cancers is usually very difficult, both because of the limited volume of RNA obtainable from the tissues and the many technical difficulties of RNA...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 1997-09, Vol.57 (17), p.3792-3797 |
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description | The search for mRNAs that are specifically expressed in cancer tissues is important for gene diagnosis and therapy. However, finding such mRNAs in human cancers is usually very difficult, both because of the limited volume of RNA obtainable from the tissues and the many technical difficulties of RNA analysis. To address these problems, the present study compared mRNA from thyroid cancer tissues with those from normal and benign tissues by reverse transcription-PCR using two degenerate primers. Amplified cDNAs were separated by electrophoresis with nondenaturing acrylamide gel, then three bands that are increased in cancer tissues were selected, reamplified by PCR, and cloned into T-vector. One of the bands was determined by sequencing analysis to be oncofetal fibronectin. The expression of oncofetal fibronectin mRNA in benign and malignant tissues was examined by Northern blot and reverse transcription-PCR using specific primers of its cDNA sequence, and its increased expression was observed only in papillary and anaplastic carcinomas. Thus, the present method rapidly detected specific mRNAs in cancer tissues, and one of these, oncofetal fibronectin mRNA, is a good target for gene diagnosis of papillary carcinoma. |
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However, finding such mRNAs in human cancers is usually very difficult, both because of the limited volume of RNA obtainable from the tissues and the many technical difficulties of RNA analysis. To address these problems, the present study compared mRNA from thyroid cancer tissues with those from normal and benign tissues by reverse transcription-PCR using two degenerate primers. Amplified cDNAs were separated by electrophoresis with nondenaturing acrylamide gel, then three bands that are increased in cancer tissues were selected, reamplified by PCR, and cloned into T-vector. One of the bands was determined by sequencing analysis to be oncofetal fibronectin. The expression of oncofetal fibronectin mRNA in benign and malignant tissues was examined by Northern blot and reverse transcription-PCR using specific primers of its cDNA sequence, and its increased expression was observed only in papillary and anaplastic carcinomas. Thus, the present method rapidly detected specific mRNAs in cancer tissues, and one of these, oncofetal fibronectin mRNA, is a good target for gene diagnosis of papillary carcinoma.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 9288789</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Adenoma - chemistry ; Adenoma - genetics ; Base Sequence ; Biological and medical sciences ; Blotting, Northern ; Carcinoma, Papillary - chemistry ; Carcinoma, Papillary - genetics ; DNA Primers ; Endocrinopathies ; Humans ; Malignant tumors ; Medical sciences ; Molecular Sequence Data ; Polymerase Chain Reaction - methods ; RNA, Messenger - analysis ; RNA, Neoplasm - analysis ; Thyroid Gland - chemistry ; Thyroid Neoplasms - chemistry ; Thyroid Neoplasms - genetics ; Thyroid. 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However, finding such mRNAs in human cancers is usually very difficult, both because of the limited volume of RNA obtainable from the tissues and the many technical difficulties of RNA analysis. To address these problems, the present study compared mRNA from thyroid cancer tissues with those from normal and benign tissues by reverse transcription-PCR using two degenerate primers. Amplified cDNAs were separated by electrophoresis with nondenaturing acrylamide gel, then three bands that are increased in cancer tissues were selected, reamplified by PCR, and cloned into T-vector. One of the bands was determined by sequencing analysis to be oncofetal fibronectin. The expression of oncofetal fibronectin mRNA in benign and malignant tissues was examined by Northern blot and reverse transcription-PCR using specific primers of its cDNA sequence, and its increased expression was observed only in papillary and anaplastic carcinomas. Thus, the present method rapidly detected specific mRNAs in cancer tissues, and one of these, oncofetal fibronectin mRNA, is a good target for gene diagnosis of papillary carcinoma.</description><subject>Adenoma - chemistry</subject><subject>Adenoma - genetics</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Carcinoma, Papillary - chemistry</subject><subject>Carcinoma, Papillary - genetics</subject><subject>DNA Primers</subject><subject>Endocrinopathies</subject><subject>Humans</subject><subject>Malignant tumors</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>Polymerase Chain Reaction - methods</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Neoplasm - analysis</subject><subject>Thyroid Gland - chemistry</subject><subject>Thyroid Neoplasms - chemistry</subject><subject>Thyroid Neoplasms - genetics</subject><subject>Thyroid. 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Thyroid axis (diseases)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAKANO, T</creatorcontrib><creatorcontrib>MATSUZUKA, F</creatorcontrib><creatorcontrib>SUMIZAKI, H</creatorcontrib><creatorcontrib>KUMA, K</creatorcontrib><creatorcontrib>AMINO, N</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAKANO, T</au><au>MATSUZUKA, F</au><au>SUMIZAKI, H</au><au>KUMA, K</au><au>AMINO, N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid detection of specific messenger RNAs in thyroid carcinomas by reverse transcription-PCR with degenerate primers : Specific expression of oncofetal fibronectin messenger RNA in papillary carcinoma</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>57</volume><issue>17</issue><spage>3792</spage><epage>3797</epage><pages>3792-3797</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>The search for mRNAs that are specifically expressed in cancer tissues is important for gene diagnosis and therapy. However, finding such mRNAs in human cancers is usually very difficult, both because of the limited volume of RNA obtainable from the tissues and the many technical difficulties of RNA analysis. To address these problems, the present study compared mRNA from thyroid cancer tissues with those from normal and benign tissues by reverse transcription-PCR using two degenerate primers. Amplified cDNAs were separated by electrophoresis with nondenaturing acrylamide gel, then three bands that are increased in cancer tissues were selected, reamplified by PCR, and cloned into T-vector. One of the bands was determined by sequencing analysis to be oncofetal fibronectin. The expression of oncofetal fibronectin mRNA in benign and malignant tissues was examined by Northern blot and reverse transcription-PCR using specific primers of its cDNA sequence, and its increased expression was observed only in papillary and anaplastic carcinomas. Thus, the present method rapidly detected specific mRNAs in cancer tissues, and one of these, oncofetal fibronectin mRNA, is a good target for gene diagnosis of papillary carcinoma.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>9288789</pmid><tpages>6</tpages></addata></record> |
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subjects | Adenoma - chemistry Adenoma - genetics Base Sequence Biological and medical sciences Blotting, Northern Carcinoma, Papillary - chemistry Carcinoma, Papillary - genetics DNA Primers Endocrinopathies Humans Malignant tumors Medical sciences Molecular Sequence Data Polymerase Chain Reaction - methods RNA, Messenger - analysis RNA, Neoplasm - analysis Thyroid Gland - chemistry Thyroid Neoplasms - chemistry Thyroid Neoplasms - genetics Thyroid. Thyroid axis (diseases) |
title | Rapid detection of specific messenger RNAs in thyroid carcinomas by reverse transcription-PCR with degenerate primers : Specific expression of oncofetal fibronectin messenger RNA in papillary carcinoma |
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